18-19 September 2018 in Cologne – Germany

OBJECTIVES

• Implementation of GMP in an excipient manufacturing site
• Qualification and auditing of suppliers
• Analytical data and certificates of analysis for excipients
• The European Pharmacopoeia’s General Methods Modernisation Programme
• USP – Strategies and Opportunities for Excipient Standard Setting
• Particulate matter in pharmaceutical starting materials and drug products
• Regulatory and technical challenges for excipients in parenteral formulations
• Formulation topics

WORKSHOPS

This year again, we offer you to arrange your individual conference focus

(Workshops will run in parallel two times. You will have the opportunity to participate in 2 workshops.)

• How to implement appropriate GMPs in an excipients manufacturing site
  – “What brings you from ISO 9001 to “Excipient GMP”
• How to use IPEC GMP principles to manage suppliers
  – “The use IPEC Guidelines in qualification and auditing of excipient suppliers”
• Analytical data and COAs of suppliers
  – “How to enable pharma industry to outsource excipient testing to suppliers”

Connect and collaborate:

Don’t miss this opportunity to meet with colleagues and potential business partners throughout the industry.

Just click on the link and register directly online: Registration

We are looking forward to welcoming you in Cologne!